The Utility of the Oncotype DX Test for Breast Cancer Patients in an Australian Multidisciplinary Setting

被引:5
作者
Choi, Joseph Do Woong [1 ]
Hughes, T. Michael D. [1 ,2 ,3 ]
Marx, Gavin [2 ,3 ,4 ]
Boyages, John [2 ,3 ,5 ]
Rutovitz, Josie [2 ,4 ]
Hasovits, Csilla [2 ,4 ]
Parasyn, Andrew [1 ,2 ]
Edirimanne, Senarath [1 ,2 ,6 ]
Ngui, Nicholas K. [1 ,2 ,6 ]
机构
[1] Sydney Adventist Hosp, Div Surg, Sydney, NSW, Australia
[2] Sydney Adventist Hosp, Breast Multidisciplinary Team, Sydney, NSW, Australia
[3] Australian Natl Univ, Sydney Adventist Hosp, Clin Sch, Canberra, ACT, Australia
[4] Sydney Adventist Hosp, Dept Med Oncol, Sydney, NSW, Australia
[5] Sydney Adventist Hosp, ICON Canc Ctr, Sydney, NSW, Australia
[6] Univ Sydney, Sydney, NSW, Australia
关键词
ASSAY; RECURRENCE;
D O I
10.1155/2022/1199245
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction. The Oncotype DX test is a genomic assay that generates a Recurrence Score (RS) predicting the 10-year risk of recurrence and response to adjuvant chemotherapy in ER+/HER2- breast cancer patients. The aims were to determine breast cancer distant recurrence and correlate with adjuvant chemoendocrine prescribing patterns based on the Oncotype DX recurrence score. Methods. We conducted a retrospective single-institution case series of 71 patients who had Oncotype DX assay testing after definitive surgery between 2012 and 2016. Both node-positive and node-negative patients were included. Patients were divided into Oncotype DX low risk (RS < 11) (n = 10, 14%), intermediate risk (RS 11-25) (n = 45, 63%), and high risk (RS > 25) (n = 16, 23%). Median follow-up was 6.1 years (range 4-8.9 years). Adjuvant treatment regimens and oncological outcomes were determined. Results. Mean age at diagnosis was 56 years (range, 33-77). Invasive ductal carcinoma (IDC) accounted for the majority (87%), with most tumors measuring between 10-20 mm (52%). 48% of the cohort were node positive. 15 of 16 high-risk patients (94%) received chemotherapy. 96% of intermediate-risk patients received endocrine therapy alone, one patient received chemoendocrine therapy (2%), and one declined systemic therapy (2%). In the low-risk group, 100% received endocrine therapy only. The high-risk group had the lowest mean ER% (P < 0.05), greatest mean mitotic rate (P < 0.05), and greatest proportion of Ki67% > 14. Five patients developed distant recurrence (7%): three from the intermediate-risk group (7%), one from the low-risk group (10%), and one from the high-risk group (6%). Conclusion. This is the first Australian study reporting the experience with medium-term recurrence outcomes of using the Oncotype DX assay in breast cancer. Chemotherapy was rarely given for patients with low-to-intermediate RS and always offered in high RS. This pattern of prescribing was associated with low rates of distant recurrence. National funding models should be considered.
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